4-Chloro-2-fluoro-3-methoxyphenylboronic acid

98%

Reagent Code: #90624
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CAS Number 944129-07-1

science Other reagents with same CAS 944129-07-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.39 g/mol
Formula C₇H₇BClFO₃
badge Registry Numbers
MDL Number MFCD1701574
thermostat Physical Properties
Melting Point 246-249°C
Boiling Point 487.6±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.40±0.1 g/cm3
Storage 2-8°C

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the production of biologically active compounds, such as drug candidates, due to its ability to introduce specific functional groups into molecular frameworks. Its unique structure, combining chloro, fluoro, and methoxy substituents, allows for precise modifications in target molecules, enhancing their properties or efficacy. Additionally, it is employed in the development of organic electronic materials, where its boronic acid group facilitates the creation of conjugated systems for use in sensors, OLEDs, or other electronic devices.

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Test Parameter Specification
Appearance White Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,340.00
inventory 1g
10-20 days ฿3,510.00
inventory 5g
10-20 days ฿10,900.00

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4-Chloro-2-fluoro-3-methoxyphenylboronic acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the production of biologically active compounds, such as drug candidates, due to its ability to introduce specific functional groups into molecular frameworks. Its unique structure, combining chloro, fluoro, and methoxy substituents, allows for precise modifications in target molecules, enhancing their properties or efficacy. Additionally, it is employed in the development of organic electronic materials, where its boronic acid group facilitates the creation of conjugated systems for use in sensors, OLEDs, or other electronic devices.
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